Detalhe da pesquisa
1.
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
Eur Heart J
; 43(45): 4707-4718, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35751511
2.
Early sarcomere and metabolic defects in a zebrafish pitx2c cardiac arrhythmia model.
Proc Natl Acad Sci U S A
; 116(48): 24115-24121, 2019 11 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31704768
3.
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.
Eur Heart J
; 42(44): 4523-4534, 2021 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34338756
4.
Potential Influence of Risk Factor Control on the Association Between Lipoprotein(a) and Atherosclerotic Cardiovascular Disease.
Arterioscler Thromb Vasc Biol
; 2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38660805
5.
Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT.
Circ Res
; 131(10): 862-865, 2022 10 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36205134
6.
Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality.
Genet Med
; 19(5): 521-528, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27711072
7.
A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression.
N Engl J Med
; 379(18): 1780-1781, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30380381
8.
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.
Eur Heart J
; 36(37): 2523-9, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26159999
9.
Association of DIO2 and MCT10 Polymorphisms With Persistent Symptoms in LT4-Treated Patients in the UK Biobank.
J Clin Endocrinol Metab
; 109(2): e613-e622, 2024 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37740545
10.
Loss of Cardiac Splicing Regulator RBM20 Is Associated With Early-Onset Atrial Fibrillation.
JACC Basic Transl Sci
; 9(2): 163-180, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38510713
11.
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis.
Nat Genet
; 56(5): 827-837, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38632349
12.
Association of PCSK9 Loss-of-Function Variants With Risk of Heart Failure.
JAMA Cardiol
; 8(2): 159-166, 2023 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36542369
13.
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.
Nat Genet
; 55(3): 399-409, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36658437
14.
Effect of Loss-of-Function Genetic Variants in PCSK9 on Glycemic Traits, Neurocognitive Impairment, and Hepatobiliary Function.
Diabetes Care
; 45(1): 251-254, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34758978
15.
Association of Common and Rare Genetic Variation in the 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Gene and Cataract Risk.
J Am Heart Assoc
; 11(12): e025361, 2022 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35703387
16.
Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.
Front Genet
; 13: 806429, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35154276
17.
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Nat Commun
; 13(1): 5144, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36050321
18.
Explaining deep neural networks for knowledge discovery in electrocardiogram analysis.
Sci Rep
; 11(1): 10949, 2021 05 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34040033
19.
DeepFake electrocardiograms using generative adversarial networks are the beginning of the end for privacy issues in medicine.
Sci Rep
; 11(1): 21896, 2021 11 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34753975
20.
Association of Variants Near the Bradykinin Receptor B2 Gene With Angioedema in Patients Taking ACE Inhibitors.
J Am Coll Cardiol
; 78(7): 696-709, 2021 08 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34384552